OMRON 3 SERIES UPPER ARM BLOOD PRESSURE MONITOR BP710N

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2019-08-01 for OMRON 3 SERIES UPPER ARM BLOOD PRESSURE MONITOR BP710N manufactured by Omron Healthcare Co., Ltd..

MAUDE Entry Details

Report Number8030245-2019-00001
MDR Report Key8849261
Report SourceCOMPANY REPRESENTATIVE,CONSUM
Date Received2019-08-01
Date of Report2019-07-15
Date of Event2019-06-25
Date Mfgr Received2019-09-05
Device Manufacturer Date2016-10-13
Date Added to Maude2019-08-01
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. TOMOJI ZUKAWA
Manufacturer Street53 KUNOTSUBO TERADO-CHO
Manufacturer CityMUKO-CITY, KYOTO 6170002
Manufacturer CountryJA
Manufacturer Postal6170002
Manufacturer G1OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD
Manufacturer StreetNO.28 VSIP II, ST. 2, VIETNAM-SINGAPORE INDUS. PARK
Manufacturer CityHOA PHU THU DAU MOT CITY, 820000
Manufacturer CountryVM
Manufacturer Postal Code820000
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOMRON 3 SERIES UPPER ARM BLOOD PRESSURE MONITOR
Generic NameBLOOD PRESSURE MONITOR,
Product CodeDXN
Date Received2019-08-01
Returned To Mfg2019-09-02
Model NumberBP710N
Catalog NumberBP710N
Lot Number20161014485VG
OperatorLAY USER/PATIENT
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerOMRON HEALTHCARE CO., LTD.
Manufacturer Address53 KUNOTSUBO TERADO-CHO MUKO-CITY, KYOTO 6170002 JA 6170002


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2019-08-01

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